Canonical Allele Identifier: CA481318563

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153897G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760119G>A , CM000674.2:g.101760119G>A	GRCh38
NC_000012.11:g.102153897G>A , CM000674.1:g.102153897G>A	GRCh37
NC_000012.10:g.100678028G>A	NCBI36
NG_021243.1:g.75749C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3160C>T MANE Select	ENSP00000299314.7:p.Leu1054=
ENST00000299314.11:c.3160C>T	ENSP00000299314.7:p.Leu1054=
ENST00000549194.1:n.26C>T
NM_024312.4:c.3160C>T	NP_077288.2:p.Leu1054=
XM_006719593.2:c.3160C>T	XP_006719656.1:p.Leu1054=
XM_011538731.1:c.3079C>T	XP_011537033.1:p.Leu1027=
XM_006719593.3:c.3160C>T	XP_006719656.1:p.Leu1054=
XM_011538731.2:c.3079C>T	XP_011537033.1:p.Leu1027=
XM_017019961.1:c.2944C>T	XP_016875450.1:p.Leu982=
XM_017019962.2:c.1933C>T	XP_016875451.1:p.Leu645=
NM_024312.5:c.3160C>T MANE Select	NP_077288.2:p.Leu1054=